Ireland
--:--IST
Recruiting Not applicable

Effectiveness of Individualized Pelvic Floor Muscle Rehabilitation in Addition to Standard Urotherapy and Alarm Therapy in Children With Primary Monosymptomatic Nocturnal Enuresis

NCT07890194 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-31
Last updated
2026-10-22

Condition(s) studied

Primary Monosymptomatic Nocturnal Enuresis

Investigational drug(s) / intervention(s)

Standard urotherapy, Alarm therapyStandard urotherapy, Alarm therapy, Individualized pelvic floor muscle rehabilitation

Standard urotherapy, Alarm therapy: Participants will receive standard urotherapy and alarm therapy for 12 weeks.

Standard urotherapy, Alarm therapy, Individualized pelvic floor muscle rehabilitation: Participants will receive standard urotherapy, alarm therapy, and pelvic floor muscle rehabilitation for 12 weeks.

Study summary

This study will evaluate whether adding individualized pelvic floor muscle rehabilitation to standard urotherapy and alarm treatment improves bedwetting in children aged 5-18 years with primary monosymptomatic nocturnal enuresis.

Participants will be randomly assigned to two groups. Both groups will receive standard urotherapy and alarm treatment. One group will also receive pelvic floor muscle rehabilitation for 12 weeks. The study will compare dry nights, alarm activations, and changes in pelvic floor muscle function between the groups.

Eligibility

Sex
ALL
Min age
5 Years
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of primary monosymptomatic nocturnal enuresis (PMNE) according to the International Children's Continence Society (ICCS) diagnostic criteria. * Age between 5 and 18 years. * Willingness to participate in the study and provision of written informed consent by a parent or legal guardian. * Recommendation of enuresis alarm therapy as a first-line treatment. Exclusion Criteria: * Presence of cognitive or intellectual impairment. * Enuresis attributable to anatomical or neurological causes. * Receipt of nonpharmacological treatment for enuresis, such as standard urotherapy, alarm therapy, pelvic floor muscle training, or electrical stimulation, within the preceding six months.

Primary outcome measure(s)

  • Number of Dry Nights — Baseline and weeks 4, 8, and 12.
    The number of nights without involuntary urine leakage during sleep will be recorded by parents using an enuresis diary.
  • Number of Enuresis Alarm Activations — Baseline and weeks 4, 8, and 12.
    The number of moisture-triggered enuresis alarm activations during sleep will be recorded by parents using an enuresis diary.

Trial sites (1)

FacilityCityRegionStatus
Hacettepe University Ankara Ankara Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07890194 on ClinicalTrials.gov ↗ ← All trials in Turkey